527 recalls tagged with “adult product”.
Cardinal Health recalled all lots of Salem Sump stomach tubes on September 18, 2025. The recall affects tubes with product codes 264929, 264945, and others due to complaints of valve breakage. Patients and healthcare providers should stop using the devices immediately.
Goyal Group recalled 293 sets of aluminium cookware on September 18, 2025. The products contain elevated levels of lead, posing a health risk. Consumers should stop using these items immediately and contact the company for a refund.
B BRAUN MEDICAL recalled its PERIFIX FX Continuous Epidural Anesthesia Set on September 18, 2025. The recall affects a potential defect in the catheter connector lid position. This high-risk issue could impact patient safety in healthcare settings across the country.
Cardinal Health 200 recalled Salem Sump PVC gastroduodenal tubes on September 18, 2025. The recall affects all lots sold worldwide due to complaints of Anti-Reflux Valve breakage. Patients and healthcare providers must stop using the devices immediately.
Cardinal Health 200 recalled Salem Sump silicone dual lumen stomach tubes on September 18, 2025. The recall affects all lots due to complaints of Anti-Reflux Valve breakage during use. Patients and healthcare providers should stop using the devices immediately.
Glenmark Pharmaceuticals Inc. recalled 13,824 tubes of Azelaic Acid Gel on September 17, 2025. The recall stems from market complaints regarding a gritty texture. Consumers should stop using the product immediately and contact their healthcare provider.
Percussionaire recalled 59,160 Phasitron 5 In-Line Valves on September 17, 2025. The valves may leak when used with ventilators, posing a high risk of respiratory failure. Consumers should stop using the product immediately and follow recall instructions.
IntegraDose Compounding Services LLC recalled 853 bags of Oxytocin 30 Units/500 mL on September 16, 2025. Testing revealed these IV bags contain no oxytocin, posing serious health risks. The recall affects products distributed nationwide in the USA.
Alcon Research LLC recalled 28,323 CONSTELLATION ULTRAVIT and HYPERVIT devices on September 15, 2025, due to a high hazard risk. The recall affects products distributed worldwide, including multiple states in the U.S. and several countries.
American Health Packaging recalled 360 cartons of Carbamazepine Extended-Release Tablets on September 15, 2025. The tablets fail to meet dissolution specifications, posing a risk to patients. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Graviti Pharmaceuticals recalled 46,512 bottles of Bupropion Hydrochloride Extended-Release Tablets on September 15, 2025. The recall stems from failed tablet specifications that could affect safety and efficacy. The product was distributed to pharmacies nationwide.
Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.
Private Label Skin Care recalled its 7 oz Acne Treatment on September 12, 2025. Elevated levels of benzene prompted the recall, classified as Class II. The affected product was distributed in California and Georgia only.
Private Label Skin Care recalled its Micronized BPO Gel Cleanser 10% on September 12, 2025. Elevated benzene levels prompted the recall in California and Georgia. Consumers must stop using the product immediately and seek guidance from healthcare providers.
Private Label Skin Care recalled 125 units of ARTISAN OF SKIN Benzoyl Peroxide 10% on September 12, 2025. Elevated benzene levels prompted the recall in California and Georgia. Consumers should stop using the product immediately and seek guidance.
GE HealthCare recalled 54 nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been transported without proper detector support. This issue poses a high risk of detector falls, potentially leading to serious injuries.
Shanghai United Imaging Healthcare Co., Ltd. recalled 11 units of its uCT 760 MD Computed Tomography X-ray System on September 12, 2025. The recall addresses a serious hazard where third-party outer covers can become trapped between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must stop using the device immediately and follow recall directives
Blueroot Health recalled Bariatric Fusion Iron Multivitamins on September 11, 2025, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating federal safety standards. Consumers should stop using the product immediately and seek replacement caps.
Olympus Corporation of the Americas recalled 1,473 EVIS EXERA II Bronchoscopes on September 11, 2025. The recall addresses critical updates to the instructions for use when combined with laser and coagulation therapies. Healthcare professionals must stop using the device immediately and follow the manufacturer's instructions.
Harris Teeter recalled 83 units of Cinnamon Texas Toast on September 11, 2025. The recall occurred due to undeclared milk in the ingredient statement. Consumers in DC, DE, FL, GA, MD, NC, SC, and VA should check their products.